JPH02227116A - Composition for drying - Google Patents
Composition for dryingInfo
- Publication number
- JPH02227116A JPH02227116A JP4884989A JP4884989A JPH02227116A JP H02227116 A JPH02227116 A JP H02227116A JP 4884989 A JP4884989 A JP 4884989A JP 4884989 A JP4884989 A JP 4884989A JP H02227116 A JPH02227116 A JP H02227116A
- Authority
- JP
- Japan
- Prior art keywords
- deliquescent
- polyalkylene glycol
- deliquescent salts
- drying
- hydrophilic polymer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 17
- 238000001035 drying Methods 0.000 title claims abstract description 10
- 150000003839 salts Chemical class 0.000 claims abstract description 33
- 229920001515 polyalkylene glycol Polymers 0.000 claims abstract description 23
- 239000002245 particle Substances 0.000 claims abstract description 20
- 229920001477 hydrophilic polymer Polymers 0.000 claims abstract description 15
- 150000002148 esters Chemical class 0.000 claims description 20
- 239000011247 coating layer Substances 0.000 claims description 6
- 239000004615 ingredient Substances 0.000 claims 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 abstract description 15
- 239000001110 calcium chloride Substances 0.000 abstract description 15
- 229910001628 calcium chloride Inorganic materials 0.000 abstract description 15
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 abstract description 4
- 239000003795 chemical substances by application Substances 0.000 abstract description 3
- 235000014113 dietary fatty acids Nutrition 0.000 abstract description 3
- 239000000194 fatty acid Substances 0.000 abstract description 3
- 229930195729 fatty acid Natural products 0.000 abstract description 3
- 150000004665 fatty acids Chemical class 0.000 abstract description 3
- 239000002202 Polyethylene glycol Substances 0.000 abstract description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract description 2
- 150000001342 alkaline earth metals Chemical class 0.000 abstract description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 abstract description 2
- 239000002736 nonionic surfactant Substances 0.000 abstract description 2
- 229920001223 polyethylene glycol Polymers 0.000 abstract description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 239000000843 powder Substances 0.000 description 21
- 239000000047 product Substances 0.000 description 20
- 229920000642 polymer Polymers 0.000 description 13
- 238000010521 absorption reaction Methods 0.000 description 11
- 239000007788 liquid Substances 0.000 description 9
- 229920002401 polyacrylamide Polymers 0.000 description 7
- 239000000499 gel Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 229920000881 Modified starch Polymers 0.000 description 5
- 229920002472 Starch Polymers 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- 239000002274 desiccant Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 5
- 239000008107 starch Substances 0.000 description 5
- 235000019698 starch Nutrition 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229920006319 cationized starch Polymers 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 235000019426 modified starch Nutrition 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- 150000004683 dihydrates Chemical group 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000004368 Modified starch Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 229910001514 alkali metal chloride Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- LLSDKQJKOVVTOJ-UHFFFAOYSA-L calcium chloride dihydrate Chemical compound O.O.[Cl-].[Cl-].[Ca+2] LLSDKQJKOVVTOJ-UHFFFAOYSA-L 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- SHFGJEQAOUMGJM-UHFFFAOYSA-N dialuminum dipotassium disodium dioxosilane iron(3+) oxocalcium oxomagnesium oxygen(2-) Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[Na+].[Na+].[Al+3].[Al+3].[K+].[K+].[Fe+3].[Fe+3].O=[Mg].O=[Ca].O=[Si]=O SHFGJEQAOUMGJM-UHFFFAOYSA-N 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- -1 etc.) Polymers 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Drying Of Gases (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、乾燥主剤である潮解性塩類の液状化を防止し
た乾燥用組成物に関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a drying composition that prevents liquefaction of deliquescent salts as a main drying agent.
従来技術
塩化カルシウム等の潮解性塩類は、吸湿性に優れるため
、乾燥剤として古くから使用されている。BACKGROUND OF THE INVENTION Deliquescent salts such as calcium chloride have long been used as desiccant agents because of their excellent hygroscopicity.
しかし、このような潮解性塩類は、吸湿に伴って液状化
するため、取り扱い難く、使用範囲に限度があった。However, since such deliquescent salts liquefy as they absorb moisture, they are difficult to handle and have a limited range of use.
そこで、このような潮解性塩類の吸湿能を害することな
く、液状化を防止する方法が種々検討されており、例え
ば、特公昭60−28531号公報には、潮解性塩類と
特定の親木性ポリマー、溶融又は溶解することなく、粉
末もしくは粒状物で機械的に混合して使用することが提
案されている。Therefore, various methods have been studied to prevent liquefaction without impairing the hygroscopic ability of deliquescent salts. For example, Japanese Patent Publication No. 60-28531 discloses that It has been proposed to use the polymers without melting or dissolving them, mechanically mixing them in powders or granules.
しかし、このような方法では、潮解性塩類と親木性ポリ
マーを、単に混合しているため、次のよな欠点があり、
実用性ある製品を得ることは困難であった。However, since this method simply mixes deliquescent salts and wood-philic polymers, it has the following drawbacks:
It was difficult to obtain a practical product.
+11 共に粉末もしくは粒状物である、潮解性塩類
と親水性ポリマーを、均質に混合することは困難である
。均一に混合するためには、使用する潮解性塩類の粒径
に応じて親木性ポリマーを適度の大きさに造粒する必要
がある。+11 It is difficult to homogeneously mix deliquescent salts and hydrophilic polymers, both of which are powders or granules. In order to mix uniformly, it is necessary to granulate the wood-philic polymer to an appropriate size depending on the particle size of the deliquescent salt used.
(2)仮に、親水性ポリマーを適度の大きさに造粒して
、一応潮解性塩類と混合できるようにしたとしても、潮
解性塩類と異質の親水性ポリマーは分離し易く、その混
合物を包装するまでの輸送工程において分離が始まり、
最終製品の均質性を確保することは困難である。(2) Even if the hydrophilic polymer is granulated to an appropriate size so that it can be mixed with the deliquescent salts, the deliquescent salts and the different hydrophilic polymer will easily separate, and the mixture will not be packaged. Separation begins during the transportation process until
It is difficult to ensure homogeneity of the final product.
(3)上記fil(21の結果として、包装単位毎の吸
湿性能及び潮解液のゲル化能にバラツキが大きく、均質
な製品を得難く、不良品が発生する危険性が大である。(3) As a result of the above fil (21), there are large variations in the moisture absorption performance and gelling ability of the deliquescent liquid for each packaging unit, making it difficult to obtain a homogeneous product and increasing the risk of producing defective products.
発明が解決しようとする課題
本発明は、このような従来法の欠点を解消し、潮解性塩
類の液状化を安定して防止し、吸湿性能及び潮解液のゲ
ル化能にバラツキのない、扱い易い乾燥用組成物を提供
することを課題とする。Problems to be Solved by the Invention The present invention solves the drawbacks of such conventional methods, stably prevents liquefaction of deliquescent salts, and provides a method for handling with no variation in moisture absorption performance and gelling ability of deliquescent liquid. An object of the present invention is to provide a composition for easy drying.
課題を解決するための手段
本発明の乾燥用組成物は、乾燥主剤である潮解性塩類の
粒子表面にポリアルキレングリコールジアルキルエステ
ルのコーティング層を設け、このコーティング層に粉末
状親水性ポリマーを付着せしめてなることを特徴とする
。Means for Solving the Problems The drying composition of the present invention provides a coating layer of polyalkylene glycol dialkyl ester on the surface of particles of deliquescent salts as a main drying agent, and adheres a powdery hydrophilic polymer to this coating layer. It is characterized by being
本発明の組成物は、このように潮解性塩類の粒子表面に
、バインダー効果を有し、しかも吸水性に優れたポリア
ルキレングリコールジアルキルエステルを介して、粉末
状親水性ポリマーを付着しているため、ゲル化成分の分
離が防止され、吸湿性及び潮解液のゲル化能共に優れた
、均質で扱い易い製品が得られる。In the composition of the present invention, the powdery hydrophilic polymer is attached to the surface of the deliquescent salt particles via the polyalkylene glycol dialkyl ester, which has a binder effect and has excellent water absorption. Separation of gelling components is prevented, and a homogeneous and easy-to-handle product with excellent hygroscopicity and gelling ability of deliquescent liquid can be obtained.
本発明において、潮解性塩類粒子表面にポリアルキレン
グリコールジアルキルエステルをコティングする方法は
特に限定されないが、一般に、ポリアルキレングリコー
ルジアルキルエステルを、その融点以上の温度で潮解性
塩類と混合して、粒子表面に展着せしめた後、冷却して
固着せしめるのが好ましい。In the present invention, the method for coating the surface of the deliquescent salt particles with the polyalkylene glycol dialkyl ester is not particularly limited, but generally, the polyalkylene glycol dialkyl ester is mixed with the deliquescent salt at a temperature equal to or higher than its melting point, and the particle surface is coated with the polyalkylene glycol dialkyl ester. It is preferable to spread the film on the film and then cool it to solidify it.
ポリアルキレングリコールジアルキルエステルは、それ
自体水分を吸収し、ゲル化する成分として、潮解性塩類
の液化防止能を有するが、同時に、適度の粘着力を有す
るため、潮解性塩類と付加的なゲル化成分(粉末状親水
性ポリマー)を一体化する接着剤としても効果的に機能
し、潮解性塩類を大気中に直接露出することなく、安定
した乾燥用組成物の提供が可能となる。Polyalkylene glycol dialkyl ester itself has the ability to prevent deliquescent salts from liquefying as a component that absorbs water and gels, but at the same time, it has a moderate adhesive strength, so it can form additional gels with deliquescent salts. It also functions effectively as an adhesive to unite the components (powdered hydrophilic polymer), making it possible to provide a stable drying composition without directly exposing deliquescent salts to the atmosphere.
このようなポリアルキレングリコールジアルキルエステ
ルとしては、分子量2000〜20000 (好ましく
は5000〜10000)のポリエチレングリコールと
、炭素数12〜22の脂肪酸(好ましくは炭素数16〜
18を主成分とする脂肪酸)とを反応させて得られる親
水基の両末端に疎水基が結合した形の非イオン界面活性
剤の使用が好ましい。Such polyalkylene glycol dialkyl esters include polyethylene glycol having a molecular weight of 2,000 to 20,000 (preferably 5,000 to 10,000) and fatty acids having 12 to 22 carbon atoms (preferably 16 to 16 carbon atoms).
It is preferable to use a nonionic surfactant in which a hydrophobic group is bonded to both ends of a hydrophilic group obtained by reacting the surfactant with a fatty acid containing 18 as a main component.
これらは自重の5〜20倍量の水及び20χ塩化カルシ
ウム水溶液をゲル化する能力がある。These have the ability to gel 5 to 20 times their own weight of water and a 20x calcium chloride aqueous solution.
また、その融点は約40〜70℃であり、融点以上の温
度において、潮解性塩類粒子と混合すると粒子表面に粘
り気のあるコーティング層を容易に形成し、この層に粉
末状親水性ポリマーを安定して付着できる。In addition, its melting point is approximately 40 to 70°C, and when mixed with deliquescent salt particles at temperatures above the melting point, a sticky coating layer is easily formed on the particle surface, and the powdered hydrophilic polymer is stably coated in this layer. can be attached.
次に、本発明に使用する潮解性塩類には、アルカリ土類
金属又はアルカリ金属の塩化物、例えば塩化カルシウム
、塩化マグネシウム、塩化リチウム等の単体または混合
物がいずれも含まれる。最も好ましい塩類は、吸湿性が
大で安価である塩化カルシウムであり、塩化カルシウム
は無水物、2水塩いずれも使用可能である。Next, the deliquescent salts used in the present invention include alkaline earth metals or alkali metal chlorides, such as calcium chloride, magnesium chloride, lithium chloride, etc. alone or in mixtures. The most preferred salt is calcium chloride, which is highly hygroscopic and inexpensive, and both anhydrous and dihydrate forms of calcium chloride can be used.
なお、塩化カルシウムで最も安価に入手できるのは2水
塩であって、粒径分布1〜4ms+、平均粒径約311
m1のものであるが、塩化カルシウムの平均粒径が1−
一以下では、ポリアルキレングリコールジアルキルエス
テル単独でも、所望のゲル化能を有するコーティング層
を賦与でき、商品価値ある製品を得ることができる。し
かし、それより粒径が大きくなると、ポリアルキレング
リコールジアルキルエステル層単独では、十分なゲル化
能を得難<、本発明に従って、ポリアルキレングリコー
ルジアルキルエステル層上に付加的なゲル化成分として
親木性ポリマー粉末を付着させる必要かある。The cheapest calcium chloride available is dihydrate, which has a particle size distribution of 1 to 4 ms+ and an average particle size of about 311.
m1, but the average particle size of calcium chloride is 1-
When the amount is less than 1, polyalkylene glycol dialkyl ester alone can provide a coating layer having the desired gelling ability, and a product with commercial value can be obtained. However, when the particle size becomes larger than that, it becomes difficult to obtain sufficient gelling ability with the polyalkylene glycol dialkyl ester layer alone.According to the present invention, the parent resin is added as an additional gelling component on the polyalkylene glycol dialkyl ester layer. Is it necessary to attach a polymer powder?
このような潮解性塩類の表面に、ポリアルキレングリコ
ールジアルキルエステル層を介して、付着される粉末状
親水性ポリマーとしては、ポリアクリルアミド、カチオ
ン化ポリアクリルアミド、澱粉及び各種加工澱粉(エス
テル化澱粉、α化澱粉、カチオン化澱粉等)、ポリビニ
ルアルコール、ポリエチレンオキサイド、メチルセルロ
ーズ、カチオン化セルローズ等がいずれも使用できる。Powdered hydrophilic polymers attached to the surface of such deliquescent salts via a polyalkylene glycol dialkyl ester layer include polyacrylamide, cationized polyacrylamide, starch, and various modified starches (esterified starch, α (modified starch, cationized starch, etc.), polyvinyl alcohol, polyethylene oxide, methyl cellulose, cationized cellulose, etc. can be used.
これらは2種以上併用されてもよい。Two or more of these may be used in combination.
なお、高吸湿容量の製品を得るには、ポリアクリルアミ
ドの使用が特に好ましく、また、経済性を重視した場合
には、澱粉及び各種加工澱粉の使用が好ましい。In addition, in order to obtain a product with a high moisture absorption capacity, it is particularly preferable to use polyacrylamide, and when economic efficiency is important, it is preferable to use starch and various modified starches.
本発明では、ポリアルキレングリコールジアルキルエス
テル層を介して、潮解性塩類の表面に粉末状親木性ポリ
マーが付着されるため、その粉末粒子径は、どのような
ものであってもよいが、固着性及び吸湿ゲル化性能いず
れの面からも、小さい方が好ましく、一般に微粉゛束状
のものを使用するのがよい。In the present invention, since the powdery wood-philic polymer is attached to the surface of the deliquescent salt through the polyalkylene glycol dialkyl ester layer, the particle size of the powder may be any size, but From the viewpoint of both properties and hygroscopic gelling performance, the smaller the size, the better, and it is generally best to use a powder in the form of a fine powder bundle.
更に、増量剤や製造性改良の目的で、炭酸カルシウム、
ゼオライト、パーライト、ホワイトカーボン等の無機粉
体を、親木性ポリマーと共に使用してもよい。Furthermore, calcium carbonate,
Inorganic powders such as zeolite, perlite, white carbon, etc. may also be used with wood-philic polymers.
本発明において、乾燥剤組成物に、適度な吸湿ゲル化能
を付与し、かつ良好な製造性を得るためには、塩化カル
シウムとゲル化成分(ポリアルキレングリコールジアル
キルエステル及び親水性ポリマー)の比率、及び粉体成
分(塩化カルシウム、親木性ポリマー、無機粉体)とバ
インダー成分(ポリアルキレングリコールジアルキルエ
ステル)の比率を適宜調節する必要がある。In the present invention, in order to impart appropriate hygroscopic gelling ability to the desiccant composition and obtain good manufacturability, the ratio of calcium chloride to gelling components (polyalkylene glycol dialkyl ester and hydrophilic polymer) is It is necessary to adjust the ratio of the powder component (calcium chloride, wood-philic polymer, inorganic powder) and the binder component (polyalkylene glycol dialkyl ester) as appropriate.
塩化カルシウムとゲル化成分の適当な比率は、ゲル化成
分の性能によって異なるが、塩化カルシウム(2水塩)
/ゲル化成分(ポリアルキレングリコールジアルキルエ
ステル及び親水性ポリマー)の重量比が約80/20〜
80/14で潮解性塩類の液状化を防止することができ
る。The appropriate ratio of calcium chloride and gelling component varies depending on the performance of the gelling component, but calcium chloride (dihydrate)
The weight ratio of /gelling component (polyalkylene glycol dialkyl ester and hydrophilic polymer) is about 80/20 ~
80/14 can prevent liquefaction of deliquescent salts.
ゲル化成分の選定ならびに処方化に際して考慮すべき点
は、
■ 濃厚潮解液(CaC1g濃度45χ〜40χ)の吸
収ゲル化能力、
■ 希薄潮解液(CaC1g濃度25χ〜15χ)のゲ
ル化能カー製品の吸湿が飽和量に達した時の液状化防止
能力、
の二点であり、これら両方を満足するように、ゲル化成
分の選択及び処方化する必要があるが、■濃厚潮解液の
吸収ゲル化能力において、特に優れているものは、カチ
オン化ポリアクリルアミド、カチオン化澱粉、カチオン
化セルローズ等カチオン化高分子化合物であり、次いで
ポリアクリルアミド、ポリアルキレングリコールジアル
キルエステルの順に優れた効果を発揮する。なお、これ
ら以外の親木性ポリマーの濃厚潮解液ゲル化能力はかな
り低いレベルである。Points to consider when selecting and formulating gelling components are: ■ Absorption gelling ability of concentrated deliquescent liquid (CaC concentration 45χ to 40χ); ■ Gelling ability of dilute deliquescent liquid (CaC concentration 25χ to 15χ) of the car product. There are two points: the ability to prevent liquefaction when moisture absorption reaches a saturated amount, and it is necessary to select and formulate a gelling component to satisfy both of these points. In terms of performance, cationized polymer compounds such as cationized polyacrylamide, cationized starch, and cationized cellulose are particularly excellent, followed by polyacrylamide and polyalkylene glycol dialkyl ester, which exhibit excellent effects in that order. Note that the ability of other wood-loving polymers to gel a concentrated deliquescent liquid is at a considerably low level.
次に、■希薄潮解液のゲル化能力に関しては、主として
、ゲル化成分の分子量が支配因子となるが、一般に入手
し易い原料を、該能力の高い順に掲げると、
+11ポリアクリルアミド、ポリエチレンオキサイド、
メチルセルローズ、
(2)澱粉、エステル化澱粉、
(3)カチオン化セルローズ、ポリアルキレングリコー
ルジアルキルエステル、α化澱粉、(4)ポリビニルア
ルコール、カチオン化澱粉、となる。Next, ■ Regarding the gelling ability of dilute deliquescent liquid, the molecular weight of the gelling component is the main controlling factor, but the commonly available raw materials are listed in descending order of their ability: +11 polyacrylamide, polyethylene oxide,
Methyl cellulose, (2) starch, esterified starch, (3) cationized cellulose, polyalkylene glycol dialkyl ester, pregelatinized starch, (4) polyvinyl alcohol, cationized starch.
濃厚及び希薄潮解液の両方に対して優れた効果を有する
ポリアクリルアミドの利用価値は、特に大きいが、コス
ト面を考慮した場合、各種ゲル化成分の特性を勘案して
、2種以上の親木性ポリマーを適宜混合使用するのが好
ましい。The utility value of polyacrylamide, which has excellent effects on both concentrated and dilute deliquescent liquids, is particularly great, but when considering the cost aspect, considering the characteristics of various gelling components, two or more types of parent trees can be used. It is preferable to use a mixture of suitable polymers.
なお、粉体成分(塩化カルシウム、親木性ポリマー、無
機塩類)とバインダー成分(ポリアルキレングリコール
ジアルキルエステル)の適当な比率は、粉体成分の種類
、粒径などにより異なるが、重量比で約80/20〜9
376であるのが好ましい。The appropriate ratio of the powder component (calcium chloride, wood-philic polymer, inorganic salts) and binder component (polyalkylene glycol dialkyl ester) varies depending on the type of powder component, particle size, etc., but the weight ratio is approximately 80/20~9
376 is preferred.
この範囲では、未付着粉末の残留、製品粒子のブロック
化、混合釜への付着等の問題がなく、品質のよい製品を
製造できる。Within this range, there are no problems such as residual unattached powder, blocking of product particles, or adhesion to the mixing pot, and it is possible to manufacture products of good quality.
バインダー成分が過多であると、製品粉末のブロック化
、混合釜への付着等が起こり易く、逆に過少であると未
付着粉末が残留し、製品包装時の粉立ちによるヒートシ
ール性不良などの問題が発生し易い。If the binder component is too large, the product powder tends to form blocks and stick to the mixing pot, while if it is too small, unattached powder will remain, resulting in poor heat sealability due to powder dusting during product packaging. Problems are likely to occur.
塩化カルシウム及びその他粉体の粒径が大きい場合の適
当なバインダー量は粒径が小さい場合と比べて相対的に
少なくなる。When the particle size of calcium chloride and other powders is large, the appropriate amount of binder is relatively small compared to when the particle size is small.
実施例1〜6
第1表に示す処方に従って、下記の方法で乾燥組成物を
製造した。製造釜としては、加熱及び冷却が可能な31
リボンミキサーを使用し、全仕込量1500gで製造し
た。Examples 1 to 6 Dry compositions were produced according to the formulations shown in Table 1 in the following manner. As a production pot, 31 is capable of heating and cooling.
It was manufactured using a ribbon mixer with a total amount of 1500 g.
+11 塩化カルシウムを仕込み、加熱攪拌しながら
、(2) ポリアルキレングリコールジアルキルエス
テルを添加し、60〜70℃で10分間加熱攪拌した後
、(3) 粉末状親木性ポリマーを添加し、60〜7
0℃で5分間加熱攪拌し、
一複数の親木性ポリマーを使用した場合は、処方記載の
順序に従って添加したが、この添加順序は特に限定され
ない、但し、炭酸カルシウム等の無機粉体を併用する場
合、この無a粉末は最後に添加するのが好ましい−(4
) その後、45〜50℃まで撹拌冷却し、製品を取
りだす。+11 Calcium chloride was charged, and while heating and stirring, (2) polyalkylene glycol dialkyl ester was added, and after heating and stirring at 60 to 70°C for 10 minutes, (3) powdered wood-philic polymer was added, and 60 to 7
Heat and stir at 0°C for 5 minutes. When using one or more wood-loving polymers, they were added according to the order of the prescription, but the order of addition is not particularly limited. However, inorganic powders such as calcium carbonate may be used in combination. In this case, it is preferable to add this a-free powder last.
) Thereafter, the mixture is stirred and cooled to 45 to 50°C, and the product is taken out.
いずれも99%以上の収率で、微粉のない安定した粒状
品を得ることができた。In all cases, stable granular products free of fine powder were obtained with a yield of 99% or more.
実m−〜6で′た一1°の 屹
各製品の25℃、85%RHでの飽和吸湿量は、下記の
通りである。The saturated moisture absorption amount of each product at 25° C. and 85% RH is as follows.
実施例1160%
実施例2183%
実施例3169%
実施例4 170%
実施例5170%
実施例6236%
いずれの製品も、飽和吸湿時の状態は餅状ゲルで、良好
な液状化防止効果を示すものであった。Example 1 160% Example 2 183% Example 3 169% Example 4 170% Example 5 170% Example 6 236% All products are in a mochi-like gel state at saturated moisture absorption and exhibit good liquefaction prevention effects. Met.
また、飽和吸湿に到るまでの間に離液はなく、いずれ安
定した状態に維持された。In addition, there was no syneresis until saturated moisture absorption was reached, and a stable state was maintained over time.
比較例
実施例3で使用したのと同じ粒状塩化カルシウム120
0gと鱗片状のα化澱粉(粒径0.5〜3曽■)300
gを31リボンミキサー中でlO分間混合後、釜より受
器に流し出す際、10個のサンプルを任意に採取し、同
様に操作して実施例3の製造後、採取した10個のサン
プルとその飽和吸湿量及びゲル性状の比較をしたく温度
25℃、湿度85χ)。Comparative Example Granular Calcium Chloride 120 same as used in Example 3
0g and scaly pregelatinized starch (particle size 0.5-3mm) 300
After mixing g for 10 minutes in a 31 ribbon mixer and pouring it out from the pot into a receiver, 10 samples were arbitrarily collected, and the same procedure was performed as in the 10 samples collected after the production of Example 3. I would like to compare the saturated moisture absorption amount and gel properties (temperature 25°C, humidity 85χ).
その結果を第2表に示す。The results are shown in Table 2.
第2表の結果から明らかなように、本発明の実施例3で
は、非常に均一な性能の製品が得られるのに対して、単
に潮解性塩類と親水性ポリマーを混合した比較例では、
品質にバラツキのある製品しか得られず、潮解性を十分
防止できない不良品の発生が認められた。また、比較例
では、潮解性塩類と親水性ポリマーがいずれも粉末状で
存在するため、取り扱い難く、粉立ちによるポリ袋のシ
ール性不良等の問題もあった。As is clear from the results in Table 2, in Example 3 of the present invention, a product with very uniform performance was obtained, whereas in the comparative example in which a deliquescent salt and a hydrophilic polymer were simply mixed,
Products with inconsistent quality were obtained, and it was observed that some defective products were produced because deliquescence could not be sufficiently prevented. Furthermore, in the comparative example, since the deliquescent salts and the hydrophilic polymer were both present in powder form, they were difficult to handle, and there were also problems such as poor sealability of the plastic bag due to dust.
発明の効果
本発明の乾燥剤組成物は、潮解性塩類の表面をゲル化成
分でコーティングしているため、潮解性塩類の液状化が
安定して防止され、吸湿性能及び潮解液のゲル化能共に
、良好で、バラツキのない、非常に扱い易い製品となる
。包装時の粉立ちゃポリ袋のシール性不良などの危険性
もなく、常に品質の安定した製品が得られる。Effects of the Invention Since the desiccant composition of the present invention coats the surface of deliquescent salts with a gelling component, liquefaction of deliquescent salts is stably prevented, and moisture absorption performance and gelling ability of deliquescent liquids are improved. In both cases, the product is good, consistent, and extremely easy to handle. There is no risk of powder falling during packaging or poor sealing of the plastic bag, and products with stable quality can always be obtained.
特許出願人 第−工業製薬株式会社Patent applicant Dai-Kogyo Seiyaku Co., Ltd.
Claims (1)
ルキレングリコールジアルキルエステルのコーティング
層を設け、このコーティング層に粉末状親水性ポリマー
を付着させてなることを特徴とする乾燥用組成物。(1) A drying composition characterized in that a coating layer of polyalkylene glycol dialkyl ester is provided on the particle surface of a deliquescent salt as a main drying ingredient, and a powdery hydrophilic polymer is attached to this coating layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4884989A JP2673366B2 (en) | 1989-03-01 | 1989-03-01 | Drying composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4884989A JP2673366B2 (en) | 1989-03-01 | 1989-03-01 | Drying composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02227116A true JPH02227116A (en) | 1990-09-10 |
JP2673366B2 JP2673366B2 (en) | 1997-11-05 |
Family
ID=12814710
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4884989A Expired - Fee Related JP2673366B2 (en) | 1989-03-01 | 1989-03-01 | Drying composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2673366B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06262028A (en) * | 1993-03-15 | 1994-09-20 | S T Chem Co Ltd | Dehumidifying composition |
EP0718034A3 (en) * | 1994-12-21 | 1997-04-16 | Dow Corning Toray Silicone | Method of making water-repellent powders |
JP2015134342A (en) * | 2013-12-18 | 2015-07-27 | 株式会社前川製作所 | Sorption body and production method of the same |
-
1989
- 1989-03-01 JP JP4884989A patent/JP2673366B2/en not_active Expired - Fee Related
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06262028A (en) * | 1993-03-15 | 1994-09-20 | S T Chem Co Ltd | Dehumidifying composition |
EP0718034A3 (en) * | 1994-12-21 | 1997-04-16 | Dow Corning Toray Silicone | Method of making water-repellent powders |
JP2015134342A (en) * | 2013-12-18 | 2015-07-27 | 株式会社前川製作所 | Sorption body and production method of the same |
Also Published As
Publication number | Publication date |
---|---|
JP2673366B2 (en) | 1997-11-05 |
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